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Lab Technician

Job in Summit, Union County, New Jersey, 07902, USA
Listing for: Real Staffing
Full Time position
Listed on 2026-02-28
Job specializations:
  • Healthcare
  • Pharmaceutical
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

This position is responsible for executing batch manufacture, setups, cleanouts, trouble shooting, subdivisions, sampling, and inventory maintenance in the DSD kilo-lab scale facility for drug substance process development and scale-up activities, associated with production of GMP and non-GMP drug substances and intermediates.

Responsibilities
  • Serve as a key member of a dynamic, scientifically driven team dedicated to the discovery, development, and optimization of safe, scalable, and efficient chemical syntheses and processes for active pharmaceutical compounds.
  • Remaining current with required GMP training and qualifications.
  • Apply cGMP principles by following internal standard operating procedures (SOPs), work practices (WPs), and regulatory requirements.
  • Execute activities in support of day-to-day operations of the Drug Substance Development kilo-lab facility, with responsibility for GMP and non-GMP processing activities.
  • Ensure facility/equipment operations, setup, cleaning, maintenance, and calibration are completed and compliant with all relevant SOPs and regulations under the direction of kilo lab supervisor.
  • Execute and assist with batch manufacture of GMP and non-GMP processing activities by preparing and operating equipment per procedures and batch record instructions, and completing subsequent equipment and area cleaning activities per established procedures.
  • Execute experiments, batch records and documents using good Documentation Practices.
  • Responsible for executing hands on equipment and facility cleaning/sanitizations, process setups reagent and compound sampling and subdivisions.
  • Order, maintain inventory, and stock shelves for materials, consumables, standard solvents, supplies, and Personal Protective Equipment (PPE).
  • Document all activities in batch records, notebook entries, equipment cleaning and use logs, reagent/compound receipt, sampling and use logs, or other worksheets.
  • Capable of working with potentially hazardous materials in an isolator, containment, or gowned in PPE including a respirator.
  • Under general guidance assists with the procurement, installation, repair, preventative maintenance, calibration, and troubleshooting of equipment including qualification activities (IQ/OQ/PQ).
  • Assist with aspects of facility planning and scheduling.
  • Assist with maintaining and controlling inventory of raw materials, intermediates, retains, and finished APIs associated with the kilo lab facility.
  • Adhere to and sponsor all quality systems for the kilo lab area (SOPs, training, documentation, etc.) to ensure cGMP compliance with standards and regulations.
  • Ensure that kilo lab activities meet all requirements for process safety and maintain compliance with all applicable safety and environmental standards and regulations.
  • Assist with tracking performance metrics for kilo lab operations.
  • Assist all chemist and engineering staff who utilize the kilo lab area, by helping to establish and drive best practices for all unit operations and activities. Serve as a resource of scientific and technical expertise regarding scale-up and kilo-lab operations.
  • Develop and maintain effective relationships with partner areas, including Analytical Development, Quality, Drug Product Development scale-up facility, Laboratory Systems Management, Facilities group, EHS, etc. to support kilo lab activities.
  • Prepare technical reports, best practice documents, Standard Operating Procedures, work practices, publications and oral presentations related to kilo lab and project activities to enhance departmental knowledge and efficiency.
  • General understanding of Root Cause Analysis and CA/PA methodologies.
Qualifications

Skills/Knowledge

Required:

  • HS Diploma or Trade Certificate with minimum 8 years relevant experience in drug substance process development, GMP/non-GMP manufacturing, scale-up, and technology transfer in the pharmaceutical industry.
  • Associates Degree with minimum of 6 years relevant experience.
  • Bachelor of Science Degree with minimum of 4 year relevant experience, required in Chemistry/Chemical Engineering or related engineering/scientific discipline or relevant experience in lieu of degree.
  • Relevant experience in Kilo…
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